WR Medical Electronics Co.

Address: 123 North Second Street, Stillwater, Minnesota 55082-5047, USA
Phone: +1-(651)-430-1200, 800-635-1312 | Fax: +1-(651)-439-8449 | Map/Directions >>

Profile: WR Medical Electronics Co. manufactures medical devices for use in the fields of neurology and ENT field. Our Q-sweat system provides sensitive, reproducible, and non-invasive instruments of sweat rate & volume. A dynamic quantitation of sweat output from 4 sites simultaneously allows the study of resting sweat activity and persistent sweat activity. Its recordings reveal whether a sweat pattern is normal, reduced, excessive or persistent. This determines the severity of autonomic disorders and recognizes patterns related to specific syndrome. Our Silverstein facial nerve monitor stimulator preserves facial nerve function. It has a strain gauge sensor placed in the corner of the patient's mouth that detects facial contractions signified by an audible signal. It has a sterile tip probe that delivers precise amounts of current to the facial nerve during surgery. It is used in otologic procedures such as tymphanoplasty and mastoidectomy.

The company was founded in 1962, has revenues of USD 5-10 Million, has ~20 employees and is ISO 9001, CE certified.

FDA Registration Number: 2118418

23 Products/Services (Click for related suppliers)  
• Clinical Paraffin Baths
• Electrodiagnostic Testing Kits
• EMG Monitoring System
• ENT Nerve Stimulator (FDA Code: ETN / 874.1820)
A surgical nerve stimulator/locator is a device that is intended to provide electrical stimulation to the body to locate and identify nerves and to test their excitability.
• Esthesiometers (FDA Code: GXB / 882.1500)
An esthesiometer is a mechanical device which usually consists of a single rod or fiber which is held in the fingers of the physician or other examiner and which is used to determine whether a patient has tactile sensitivity.
• Hot & Cold Therapy Products, Paraffin Bath Boot & Glove
• Hot & Cold Therapy Products, Paraffin Wax Refills
• Iontophoresis Device (FDA Code: KTB / 890.5525)
An iontophoresis device is a device that is intended to use a direct current to introduce ions of soluble salts or other drugs into the body and induce sweating for use in the diagnosis of cystic fibrosis or for other uses if the labeling of the drug intended for use with the device bears adequate directions for the device's use with that drug. When used in the diagnosis of cystic fibrosis, the sweat is collected and its composition and weight are determined.
• Iontophoresis Device (FDA Code: EGJ / 890.5525)
• Medical Computer and Software (FDA Code: LNX)
• Medical Tilt Table
• Moisture Sensor
• Nerve Excitability Test Kit
• Nerve Maximal Stimulation Test Kit
• Olfactory Test Kit (FDA Code: NRK / 874.1600)
• Paraffin Bath (FDA Code: IMC / 890.5110)
A paraffin bath is a device intended for medical purposes that consists of a tub to be filled with liquid paraffin (wax) and maintained at an elevated temperature in which the patient's appendages (e.g., hands or fingers) are placed to relieve pain and stiffness.
• Paraffin Wax Bath
• Paraffin Wax Kits
• Portable Paraffin Baths
• Quantitative Sensory Testing Kit
• Sensory Nerve Tester
• Sweat Measurement Kit
• Vibration Threshold Measurement Device (FDA Code: LLN / 882.1200)

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